Bristol Laboratories Ltd
Luton, UK
18 May 2019
27 May 2019
Contract Type
Full Time

£40,000 - £45,000 per annum

Luton, Bedfordshire,

Peterlee, County Durham

About us

Bristol Laboratories Ltd is one of the leading and fastest growing pharmaceutical companies in the United Kingdom engaged in the development, manufacturing, marketing and distribution of generic medicines, as well as formulation brands. We have state-of-the art manufacturing facilities in Luton & Peterlee.

As a result of continued growth and expansion, we have an excellent opportunity to appoint Senior Quality Control Manager for our Luton and Peterlee site to lead Quality Control team.

About Job

Key Responsibilities
  • Provide leadership to the Quality Control Analyst team to ensure that appropriate methodologies and strategies are developed in support of projects and commercial activities.
  • Supporting regulatory and quality assurance activities. This will include assisting in investigation and root cause analysis of quality issues and helping to execute CAPAs.
  • Keep up-to-date with the technical literature in field of expertise in order to identify appropriate analytical tests and models
  • Schedule development of methods for current projects.
  • Support the development and continuous improvement of the company's quality management systems to maintain continued compliance
  • Ensure that the plan for releases are achieved on weekly basis.
  • Ensure GEMBAs are scheduled and executed
  • Being Inspection ready at all times.
  • Ensure analysts are trained regarding the operation of equipment and performing of new methods and/or analytical techniques as well as company policies
  • Adhere to all cGMPs, compliance/regulatory mandates and quality requirements
  • Take responsibility for designing studies and protocols and writing reports to support method development and validation
  • Complete chemical, physical or instrumental assays or tests on any pharmaceutical product, in-process material, or raw material for assigned products/projects.

About you

  • Academic achievement to Post graduate Degree level in a Science based discipline.
  • Thorough understanding of and ability to apply SOPs, GMPs, GLPs, department procedures, and controlled substance handling procedures to facilitate completion of assignments.
  • Familiar with current EU regulatory requirements for drug product manufacturing.
  • Demonstrated leadership and interpersonal skills with ability to coach and mentor personnel to consistently high standards.
  • Proven management skills, including organizational skills necessary to lead in a multi-disciplinary environment.
  • Able to develop and maintain strong working relationships with primary support functions.
  • Excellent verbal/written communication and interpersonal skills
  • Competent computer skills (Microsoft Office, Excel etc.)

This is a fantastic development opportunity for someone seeking the next step in their management career in a high profile environment. This role will interact with all levels within the business across UK & Europe.

The last date for application of this job vacancy will be 31st May 2019.

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